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Latent trajectories of adolescent antisocial behavior: Serotonin transporter linked polymorphic region (5-HTTLPR) genotype influences sensitivity to perceived parental support

机译:青少年反社会行为的潜在轨迹:血清素转运蛋白连接多态性区域(5-HTTLPR)基因型影响敏感性父母支持的敏感性

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Although prevailing theories of antisocial behavior (ASB) emphasize distinct developmental trajectories, few studies have explored gene-environment interplay underlying membership in empirically derived trajectories. To improve knowledge about the development of overt (e.g., aggression) and covert (e.g., delinquency) ASB, we tested the association of the 44-base pair promoter polymorphism in the serotonin transporter linked polymorphic region gene (5-HTTLPR), perceived parental support (e.g., closeness and warmth), and their interaction with ASB trajectories derived using latent class growth analysis in 2,558 adolescents followed prospectively into adulthood from the National Longitudinal Study of Adolescent Health. Three distinct trajectories emerged for overt (low desisting, adolescent peak, and late onset) and covert ASB (high stable, low stable, and nonoffending). Controlling for sex, parental support inversely predicted membership in the adolescent-peak overt ASB trajectory (vs. low desisting), but was unrelated to class membership for covert ASB. Furthermore, the 5-HTTLPR genotype significantly moderated the association of parental support on overt ASB trajectory membership. It is interesting that the pattern of Gene x Environment interaction differed by trajectory class: whereas short allele carriers were more sensitive to parental support in predicting the late-onset trajectory, the long/long genotype functioned as a potential "plasticity genotype" for the adolescent-peak trajectory group. We discuss these preliminary findings in the context of the differential susceptibility hypothesis and discuss the need for future studies to integrate gene-environment interplay and prospective longitudinal designs.
机译:虽然普遍的反社会行为理论(ASB)强调明显的发育轨迹,但很少有研究已经探索了基因环境在经验衍生的轨迹中的潜在成员国的相互作用。为了改善关于公开(例如,侵略)和封闭(例如,犯罪)ASB的发展的知识,我们测试了44碱基对促进剂多态性在血清素转运蛋白连接的多态性区域基因(5-HTTLPR)中的关联,感知父母支持(例如,亲密度和温暖),以及它们与在2,558名青少年使用潜在阶级增长分析的ASB轨迹的相互作用,随着青少年健康的国家纵向研究,前瞻性地进入成年。出现了公开(低停用,青少年峰值和晚发)的三个不同的轨迹,覆盖ASB(高稳定,低稳定,非官方)。控制性别,父母的支持在青少年高度ASB轨迹(VS.低停止)中的成员身份预测成员资格,但与秘密ASB的课程成员关系无关。此外,5-HTTLPR基因型显着调节父母支持与公开ASB轨迹成员的关联。有趣的是,基因X环境相互作用的模式由轨迹类别不同:而短等位基因载体对预测晚期轨迹的父母支持更敏感,但是长/长基因型作为青少年的潜在“塑性基因型”。 -peak轨迹组。我们在差异敏感假设的背景下讨论了这些初步调查结果,并讨论了未来研究的需求,以整合基因环境相互作用和预期纵向设计。

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